Serveur d'exploration sur le lymphœdème

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Stewart-Treves syndrome in a patient with elephantiasis

Identifieur interne : 00AC73 ( Main/Exploration ); précédent : 00AC72; suivant : 00AC74

Stewart-Treves syndrome in a patient with elephantiasis

Auteurs : Dafna Hallel-Halevy [Israël] ; Joseph Yerushalmi [Israël] ; Marcelo H. Grunwald [Israël] ; Ilana Avinoach [Israël] ; Sima Halevy [Israël]

Source :

RBID : ISTEX:06353E48159B8A3FD76C00BA0E8514D8F9F225A7

Descripteurs français

English descriptors

Abstract

Angiosarcoma that develops in areas of chronic lymphedema is also called Stewart-Treves syndrome. It usually appears in areas of lymphedema several years after mastectomy for breast carcinoma. Only 10% of these angiosarcomas occur in areas of chronic lymphedema as a result of another cause. We present a patient with epithelioid angiosarcoma as a rare complication of elephantiasis. (J Am Acad Dermatol 1999;41:349-50.)

Url:
DOI: 10.1016/S0190-9622(99)70385-3


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<div type="abstract" xml:lang="en">Angiosarcoma that develops in areas of chronic lymphedema is also called Stewart-Treves syndrome. It usually appears in areas of lymphedema several years after mastectomy for breast carcinoma. Only 10% of these angiosarcomas occur in areas of chronic lymphedema as a result of another cause. We present a patient with epithelioid angiosarcoma as a rare complication of elephantiasis. (J Am Acad Dermatol 1999;41:349-50.)</div>
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